@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP63985.RAyR9_0ofF1NVXj6Te3skEepwlJUNrBt_j4Or8SuEaNBs> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP63985.RAyR9_0ofF1NVXj6Te3skEepwlJUNrBt_j4Or8SuEaNBs130_head {
  this: np:hasAssertion dgn-np:NP63985.RAyR9_0ofF1NVXj6Te3skEepwlJUNrBt_j4Or8SuEaNBs130_assertion;
    np:hasProvenance dgn-np:NP63985.RAyR9_0ofF1NVXj6Te3skEepwlJUNrBt_j4Or8SuEaNBs130_provenance;
    np:hasPublicationInfo dgn-np:NP63985.RAyR9_0ofF1NVXj6Te3skEepwlJUNrBt_j4Or8SuEaNBs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP63985.RAyR9_0ofF1NVXj6Te3skEepwlJUNrBt_j4Or8SuEaNBs130_assertion a np:Assertion .
  
  dgn-np:NP63985.RAyR9_0ofF1NVXj6Te3skEepwlJUNrBt_j4Or8SuEaNBs130_provenance a np:Provenance .
  
  dgn-np:NP63985.RAyR9_0ofF1NVXj6Te3skEepwlJUNrBt_j4Or8SuEaNBs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP63985.RAyR9_0ofF1NVXj6Te3skEepwlJUNrBt_j4Or8SuEaNBs130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGNf46b7a689fe96ac6c6de87224bc9ce16 sio:SIO_000628 miriam-gene:1029, lld:C0011860;
    a sio:SIO_001122 .
}

dgn-np:NP63985.RAyR9_0ofF1NVXj6Te3skEepwlJUNrBt_j4Or8SuEaNBs130_provenance {
  dgn-np:NP63985.RAyR9_0ofF1NVXj6Te3skEepwlJUNrBt_j4Or8SuEaNBs130_assertion dcterms:description
      "[We identify T2D-associated variants in an intergenic region of chromosome 11p12, contribute to the identification of T2D-associated variants near the genes IGF2BP2 and CDKAL1 and the region of CDKN2A and CDKN2B, and confirm that variants near TCF7L2, SLC30A8, HHEX, FTO, PPARG, and KCNJ11 are associated with T2D risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:17463248;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP63985.RAyR9_0ofF1NVXj6Te3skEepwlJUNrBt_j4Or8SuEaNBs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:30+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}